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Term:Brugada syndrome 9
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Accession:DOID:0110226 term browser browse the term
Definition:A Brugada syndrome that has_material_basis_in heterozygous mutation in the KCND3 gene on chromosome 1p13. (DO)
Synonyms:exact_synonym: BRGDA9
 primary_id: OMIM:616399
 alt_id: RDO:9001381
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Brugada syndrome 9 term browser
Symbol Object Name JBrowse Chr Start Stop Reference
G Kcnd3 potassium voltage-gated channel subfamily D member 3 JBrowse link 2 207,923,775 208,140,727 RGD:7240710
G Lama4 laminin subunit alpha 4 JBrowse link 20 44,060,715 44,201,966 RGD:8554872

Term paths to the root
Path 1
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  disease 15984
    syndrome 6094
      Brugada syndrome 65
        Brugada syndrome 9 2
Path 2
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  disease 15984
    Developmental Diseases 9281
      Congenital, Hereditary, and Neonatal Diseases and Abnormalities 8095
        genetic disease 7613
          monogenic disease 5382
            autosomal genetic disease 4348
              autosomal dominant disease 2713
                Brugada syndrome 9 2
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RGD is funded by grant HL64541 from the National Heart, Lung, and Blood Institute on behalf of the NIH.